Canonical Allele Identifier: CA378890995
Gene: IFITM5 HGNC NCBI

Linked Data

gnomAD v4: 11-299418-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299418T>G , CM000673.2:g.299418T>G GRCh38
NC_000011.9:g.299418T>G , CM000673.1:g.299418T>G GRCh37
NC_000011.8:g.289418T>G NCBI36
NG_032892.1:g.5109A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.73A>C MANE Select ENSP00000372059.2:p.Thr25Pro
NM_001025295.2:c.73A>C NP_001020466.1:p.Thr25Pro
NM_001025295.3:c.73A>C MANE Select NP_001020466.1:p.Thr25Pro